arXiv subjects

B. Sundqvist

Publications and source records attributed to B. Sundqvist.

13 recordsLinked to original sources

arXiv2014

The low temperature heat capacity of solutions of methane isotopes in fullerite C60. Isotope effects

The heat capacity C(T) of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4-120 K. The contribution of CH4 molecules to the heat capacity has been separated. The contributions of CH4 and CD4 molecules to the heat capacity of the solutions (CH4)0.40C60 and (CD4)0.40C60 have been compared. It is found that above 80K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14-35 K the heat capacities of CH4 and CD4 molecules are satisfactorily described by contributions of the translational and libration vibrations, as well as the tunnel rotation for the equilibrium distribution of the nuclear spin species. The isotope effect in heat capacity of CH4 and CD4 molecules is due, mainly, the difference in the frequencies of local tranlational and libration vibrations of molecules CH4 and CD4. The contribution of the tunnel rotation of the CH4 and CD4 molecules to the heat capacities of this gases is dominant below 8 K. The isotopic effect is caused by the difference between both the conversion rates and the rotational spectra of the nuclear spin species of CH4 and CD4 molecules. The conversion rate of CH4 molecules is several times lower than that of CD4 ones. Weak features observed in the curves of heat capacity of CH4 and CD4 near 6 K and 8 K, respectively, are most likely a manifestation of first-order phase transitions in the orientational glasses of these solutions.

cond-mat.mes-hall↗

arXiv2011

The effect of O2 impurities on the low temperature radial thermal expansion of bundles of closed single-walled carbon nanotubes

The effect of oxygen impurities upon the radial thermal expansion (ar) of bundles of closed single-walled carbon nanotubes has been investigated in the temperature interval 2.2-48 K by the dilatometric method. Saturation of bundles of nanotubes with oxygen caused an increase in the positive ar-values in the whole interval of temperatures used. Also, several peaks appeared in the temperature dependence ar(T) above 20 K. The low temperature desorption of oxygen from powders consisting of bundles of single-walled nanotubes with open and closed ends has been investigated

cond-mat.mes-hall↗

arXiv2010

Quantum effects in the radial thermal expansion of bundles of single-walled carbon nanotubes doped with 4He

The radial thermal expansion (ar) of bundles of single-walled carbon nanotubes saturated with 4He impurities to the molar concentration 9.4% has been investigated in the interval 2.5-9.5 K using the dilatometric method. In the interval 2.1-3.7 K (ar) is negative and is several times higher than the negative (ar) for pure nanotube bundles. This most likely points to 4He atom tunneling between different positions in the nanotube bundle system. The excess expansion was reduced with decreasing 4He concentration.

cond-mat.mes-hall↗

arXiv2009

The effect of sorbed hydrogen on low temperature radial thermal expansion of single walled carbon nanotube bundles

The effect of a normal H2 impurity upon the radial thermal expansion (Ar) of SWNT bundles has been investigated in the interval T = 2.2-27 K using the dilatometric method. It is found that H2 saturation of SWNT bundles causes a shift of the temperature interval of the negative thermal expansion towards lower (as compared to pure CNTs) temperatures and a sharp increase in the magnitude of (Ar) in the whole range of temperatures investigated. The low temperature desorption of H2 from a powder consisting of bundles of SWNTs, open and closed at the ends, has been investigated.

cond-mat.mes-hall↗

arXiv2008

Radial thermal expansion of single-walled carbon nanotube bundles at low temperatures

The linear coefficient of the radial thermal expansion has been measured on a system of SWNT bundles in an interval of 2.2 - 120K. The measurement was performed using a dilatometer with a sensitivity of 2*10-9 cm. The cylindrical sample 7 mm high and 10 mm in diameter was obtained by compressing powder. The resulting bundles of the nanotubes were oriented perpendicular to the sample axis. The starting powder contained over 90% of SWNTs with the outer diameter 1.1 nm, the length varying within 5-30 um.

cond-mat.mtrl-sci↗

arXiv2008

The effect of the noncentral impurity-matrix interaction upon the thermal expansion and polyamorphism of solid CO-C60 solutions at low temperatures

Orientational glasses with CO molecules occupying 26% and 90% of the octahedral interstitial sites in the C60 lattice have been investigated by the dilatometric method in a temperature interval of 2.5 - 23 K. At temperatures 4 - 6 K the glasses undergo a first-order phase transition which is evident from the hysteresis of the thermal expansion and the maxima in the temperature dependences of the linear thermal expansion coefficients, and the thermalization times of the samples. The effect of the noncentral CO-C60 interaction upon the thermal expansion and the phase transition in these glasses was clarified by comparing the behavior of the properties of the CO-C60 and N2-C60 solutions.

cond-mat.dis-nn↗

arXiv2006

Low temperature heat capacity of fullerite C60 doped with nitrogen

The heat capacity Cm of polycrystalline fullerite C60 doped with nitrogen has been measured in the temperature interval 2 - 13 K. The contributions to heat capacity from translational lattice vibrations (Debye contribution), orientational vibrations of the C60 molecules (Einstein contribution) and from the motion of the N2 molecules in the octahedral cavities of the C60 lattice have been estimated. However, we could not find (beyond the experimental error limits) any indications of the first - order phase transformation that had been detected earlier in the dilatometric investigation of the orientational N2-C60 glass. A possible explanation of this fact is proposed.

cond-mat.mtrl-sci↗

arXiv2006

Thermal expansion and polyamorphism of N2 - C60 solutions

The linear thermal expansion coefficients a(T) of N2 - C60 solutions with 9.9% and 100% of the C60 lattice interstitials filled with N2 have been investigated in the interval 2.2 - 24 K. The dependence a(T) has a hysteresis suggesting co-existence of two types of orientational glasses in these solutions. The features of the glasses are compared. The characteristic times of phase transformations in the solutions and reorientation of C60 molecules have been estimated.

cond-mat.mtrl-sci↗

arXiv2004

On the polyamorphism of fullerite-based orientational glasses

The dilatometric investigation in the temperature range of 2-28K shows that a first-order polyamorphous transition occurs in the orientational glasses based on C60 doped with H2, D2 and Xe. A polyamorphous transition was also detected in C60 doped with Kr and He. It is observed that the hysteresis of thermal expansion caused by the polyamorphous transition (and, hence, the transition temperature) is essentially dependent on the type of doping gas. Both positive and negative contributions to the thermal expansion were observed in the low temperature phase of the glasses. The relaxation time of the negative contribution occurs to be much longer than that of the positive contribution. The positive contribution is found to be due to phonon and libron modes, whilst the negative contribution is attributed to tunneling states of the C60 molecules. The characteristic time of the phase transformation from the low-T phase to the high-T phase has been found for the C60-H2 system at 12K. A theoretical model is proposed to interpret these observed phenomena. The theoretical model proposed, includes a consideration of the nature of polyamorphism in glasses, as well as the thermodynamics and kinetics of the transition. A model of non-interacting tunneling states is used to explain the negative contribution to the thermal expansion. The experimental data obtained is considered within the framework of the theoretical model. From the theoretical model the order of magnitude of the polyamorphous transition temperature has been estimated. It is found that the late stage of the polyamorphous transformation is described well by the Kolmogorov law with an exponent of n=1. At this stage of the transformation, the two-dimensional phase boundary moves along the normal, and the nucleation is not important.

cond-mat.dis-nn↗

arXiv2002

Low temperature thermal expansion of pure and inert gas-doped Fullerite C60

The low temperature (2-24 K) thermal expansion of pure (single crystal and polycrystalline) C60 and polycrystalline C60 intercalated with He, Ne, Ar, and Kr has been investigated using high-resolution capacitance dilatometer. The investigation of the time dependence of the sample length variations on heating shows that the thermal expansion is determined by the sum of positive and negative contributions, which have different relaxation times. The negative thermal expansion usually prevails at helium temperatures. The positive expansion is connected with the phonon thermalization of the system. The negative expansion is caused by reorientation of the C60 molecules. It is assumed that the reorientation is of quantum character. The inert gas impurities affect very strongly the reorientation of the C60 molecules especially at liquid helium temperatures. A temperature hysteresis of the thermal expansion coefficient of Kr- and He- C60 solutions has been revealed. The hysteresis is attributed to orientational polyamorphous transformation in these systems.

cond-mat.mtrl-sci↗

arXiv2001

Band structure and transport studies on PdAl2Cl8-intercalated graphite

The 2D Fermi surface of 1st stage PdAl2Cl8 acceptor-type graphite intercalation compounds (GICs) has been investigated using the Shubnikov-de Haas (SdH) effect. One fundamental frequency is observed, the angular variation of which confirms its strongly 2D nature, as previously found through electrical conductivity measurements. The energy spectrum can be described by the 2D band structure model proposed by Blinowski et al. We obtain the following parameter values: intraplane C-C interaction energy gamma_0 = 2.7 eV, Fermi energy E_F = -1.1 eV and carrier density n_SdH= 1.1x10^27 m^-3. Some fewer details are presented on stage 2 and 3 materials.

cond-mat.mtrl-sci↗

arXiv1998

Intermolecular bond stability of C60 dimers and 2D pressure-polymerized C60

The thermal stability of C60 dimers and 2D pressure-polymerized C60 is studied using high-resolution capacitance dilatometry. The transformation of both the dimer and the polymer phases back to 'normal' C60 is excellently described by a simple thermally activated process, with activation energies of 1.75 1 0.1 eV (dimer) and 1.9 1 0.2 eV (polymer). These results are compared to previous data of 1D-polymerized C60 and photo-polymerized C60. The thermal expansivity of the 2D-polymer phase is as much as a factor of ten smaller than that of pure C60 and approaches values for diamond.

cond-mat↗

arXiv1997

From Lorentz Force on Electron to Magnus Force on Vortex, Role of Experiments

The vortex motion in a superfluid or a type II superconductor is similar to the electron motion in a magnetic field, because they both feel a transverse force. The vortex dynamics in a superconductor is a basic property of the superconductivity which remains controversial. It is also responsible for a large class of observed physical phenomena. We will examine this issue from the experimental point of view. In particular, we will compare the experiments which have set the stage to the Lorentz force and the experiments influencing our understanding of the Magnus force on vortices in superconductors.

cond-mat.supr-con↗